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Mating System and Genetic Structure Across All Known Populations of Dyckia brevifolia: A Clonal, Endemic, and Endangered Rheophyte Bromeliad

https://doi.org/10.1093/jhered/esx011
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Outgoing claims: the papers this work cites, builds on, or argues with.

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LOCAL GENETIC AND CLONAL STRUCTURE IN THE TROPICAL TERRESTRIAL BROMELIAD, AECHMEA MAGDALENAE
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The influence of seed dispersal mechanisms on the genetic structure of plant populations
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Inferring demographic processes from the genetic structure of a metapopulation of Boltonia decurrens(Asteraceae)
inferredcites →https://doi.org/10.1007/s10592-011-0183-3openalex-snapshot
Genetic diversity, genetic drift and mixed mating system in small subpopulations of Dyckia ibiramensis, a rare endemic bromeliad from Southern Brazil
inferredcites →https://doi.org/10.1007/s10682-005-0292-xopenalex-snapshot
Mating System and Clonal Architecture: A Comparative Study in Two Marine Angiosperms
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Spatiotemporal structure of genetic variation of a spreading plant metapopulation on dynamic riverbanks along the Meuse River
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Evidence for spatial structure and directional gene flow in a population of an aquatic plant, Potamogeton coloratus
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Population genetics of Dioon edule Lindl. (Zamiaceae, Cycadales): biogeographical and evolutionary implications
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.01898.xopenalex-snapshot
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Population Size, Genetic Variation, and Reproductive Success in a Rapidly Declining, Self-Incompatible Perennial (Arnica montana) in The Netherlands
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Correlation between Fitness and Genetic Diversity
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Genetic structuring of the stream lily Helmholtzia glaberrima (Philydraceae) within Toolona Creek, south-eastern Queensland
inferredcites →https://doi.org/10.1086/283106openalex-snapshot
Effect of Migration on Genetic Distance
inferredcites →https://doi.org/10.1093/aob/mch070openalex-snapshot
Genetic Variability of the Narrow Endemic Tree Antirhea aromatica Castillo-Campos & Lorence, (Rubiaceae, Guettardeae) in a Tropical Forest of Mexico
inferredcites →https://doi.org/10.1093/aob/mci125openalex-snapshot
Genetic Diversity in Fragmented Populations of Berchemiella wilsonii var. pubipetiolata (Rhamnaceae)
inferredcites →https://doi.org/10.1093/genetics/49.4.561openalex-snapshot
THE STEPPING STONE MODEL OF POPULATION STRUCTURE AND THE DECREASE OF GENETIC CORRELATION WITH DISTANCE
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STATISTICAL STUDIES ON PROTEIN POLYMORPHISM IN NATURAL POPULATIONS. III. DISTRIBUTION OF ALLELE FREQUENCIES AND THE NUMBER OF ALLELES PER LOCUS
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Genetic Diversity in Natural Populations of Piper cernuum
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Patterns of Gene Flow in Encholirium horridum L.B.Sm., a Monocarpic Species of Bromeliaceae From Brazil
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FSTAT (Version 1.2): A Computer Program to Calculate F-Statistics
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The reproductive biology and genetics of island plants
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Effects of life history traits on genetic diversity in plant species
inferredcites →https://doi.org/10.1098/rstb.2000.0740openalex-snapshot
Effects of metapopulation processes on measures of genetic diversity
inferredcites →https://doi.org/10.1111/j.0022-0477.2004.00906.xopenalex-snapshot
Dispersal phenology of hydrochorous plants in relation to discharge, seed release time and buoyancy of seeds: the flood pulse concept supported
inferredcites →https://doi.org/10.1111/j.1365-2699.2010.02331.xopenalex-snapshot
Patterns of population genetic diversity in riparian and aquatic plant species along rivers
inferredcites →https://doi.org/10.1111/j.1365-2745.2005.01048.xopenalex-snapshot
Effects of long‐distance dispersal for metapopulation survival and genetic structure at ecological time and spatial scales
inferredcites →https://doi.org/10.1111/j.1365-294x.2007.03535.xopenalex-snapshot
Standardizing methods to address clonality in population studies
inferredcites →https://doi.org/10.1111/j.1442-1984.2006.00158.xopenalex-snapshot
Consequences of hydrochory in Hibiscus
inferredcites →https://doi.org/10.1111/j.1469-1809.1949.tb02451.xopenalex-snapshot
THE GENETICAL STRUCTURE OF POPULATIONS
inferredcites →https://doi.org/10.1111/j.1523-1739.2006.00565.xopenalex-snapshot
Genetic Structure and Early Effects of Inbreeding in Fragmented Temperate Forests of a Self‐Incompatible Tree, Embothrium Coccineum
inferredcites →https://doi.org/10.1111/j.1558-5646.1969.tb03496.xopenalex-snapshot
VARIANCE OF GENE FREQUENCIES
inferredcites →https://doi.org/10.1111/j.1558-5646.1984.tb05657.xopenalex-snapshot
ESTIMATING F -STATISTICS FOR THE ANALYSIS OF POPULATION STRUCTURE
inferredcites →https://doi.org/10.1111/j.1558-5646.1989.tb05182.xopenalex-snapshot
CORRELATED MATINGS IN THE PARTIAL SELFER MIMULUS GUTTATUS
inferredcites →https://doi.org/10.1111/j.1558-5646.1993.tb01237.xopenalex-snapshot
A LIFE‐HISTORY BASED STUDY OF POPULATION GENETIC STRUCTURE: SEED BANK TO ADULTS IN PLANTAGO LANCEOLATA
inferredcites →https://doi.org/10.1111/j.1601-5223.2001.00075.xopenalex-snapshot
Genetic Diversity in Populations of Plants with Different Breeding and Dispersal Strategies in a Free-Flowing Boreal River System
inferredcites →https://doi.org/10.1111/j.1744-7429.2006.00217.xopenalex-snapshot
Genetic Variation in Fragmented Forest Stands of the Andean Oak Quercus humboldtii Bonpl. (Fagaceae)1
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Genetic differentiation, diversity, and inbreeding in the mountain monkeyflower (Mimulus caespitosus) of the Washington Cascades
inferredcites →https://doi.org/10.1146/annurev.ecolsys.34.030102.151717openalex-snapshot
Genetic Variation in Rare and Common Plants
inferredcites →https://doi.org/10.1146/annurev.ecolsys.36.091704.175539openalex-snapshot
The Evolutionary Enigma of Mixed Mating Systems in Plants: Occurrence, Theoretical Explanations, and Empirical Evidence
inferredcites →https://doi.org/10.1146/annurev.es.15.110184.000433openalex-snapshot
Ecological Determinants of Genetic Structure in Plant Populations
inferredcites →https://doi.org/10.1146/annurev.es.16.110185.002141openalex-snapshot
Gene Flow in Natural Populations
inferredcites →https://doi.org/10.1590/s0100-84042009000400008openalex-snapshot
Biologia reprodutiva da reófita Dyckia brevifolia Baker (Bromeliaceae), no Rio Itajaí-Açu, Santa Catarina, Brasil
inferredcites →https://doi.org/10.1590/s1415-47572012000600017openalex-snapshot
Genetics, evolution and conservation of Bromeliaceae
inferredcites →https://doi.org/10.2307/2446054openalex-snapshot
Microgeographic genetic structure and gene flow in Hibiscus moscheutos (Malvaceae) populations
inferredcites →https://doi.org/10.2307/2656714openalex-snapshot
Long‐distance seed dispersal in plant populations
inferredcites →https://doi.org/10.24278/2178-5031.2002142412openalex-snapshot
NÚMERO DE ÁRVORES MATRIZES E CONCEITOS GENÉTICOS NA COLETA DE SEMENTES PARA REFLORESTAMENTOS COM ESPÉCIES NATIVAS
inferredcites →https://doi.org/10.3732/ajb.1300388openalex-snapshot
Population genetics of the endemic and endangered Vriesea minarum (Bromeliaceae) in the Iron Quadrangle, Espinhaço Range, Brazil
inferredcites →https://doi.org/10.3732/ajb.93.2.206openalex-snapshot
High interpopulation genetic differentiation and unidirectional linear migration patterns in Myricaria laxiflora (Tamaricaceae), an endemic riparian plant in the Three Gorges Valley of the Yangtze River
inferredcites →https://doi.org/10.3732/ajb.94.2.151openalex-snapshot
Multiscale analysis of Hymenocallis coronaria (Amaryllidaceae) genetic diversity, genetic structure, and gene movement under the influence of unidirectional stream flow
inferredcites →https://doi.org/10.3732/ajb.94.7.1137openalex-snapshot
Hydrochory as a determinant of genetic distribution of seeds within Hibiscus moscheutos (Malvaceae) populations

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.11646/phytotaxa.729.1.1zenodo-depositor-declared
Taxonomic review of the Dyckia remotiflora complex (Bromeliaceae, Pitcairnioideae)
inferred← citeshttps://doi.org/10.2139/ssrn.4102730openalex-extracted
inferred← citeshttps://doi.org/10.1007/s00114-022-01799-5openalex-snapshot
Extranuptial nectaries in bromeliads: a new record for Pitcairnia burchellii and perspectives for Bromeliaceae
inferred← citeshttps://doi.org/10.1007/s10265-026-01710-7openalex-snapshot
The reproductive biology of Dyckia scrutor (Bromeliaceae): an endangered species endemic to Campos Rupestres
inferred← citeshttps://doi.org/10.1007/s12229-024-09310-7openalex-snapshot
The Seed Coat Structure in Bromeliaceae Juss. (Poales): Morphoanatomical Diversity and Insights Into Character Evolution
inferred← citeshttps://doi.org/10.1007/s12231-018-9414-6openalex-snapshot
Genetic Conservation of Brazilian Pine (Araucaria angustifolia) Through Traditional Land Use
inferred← citeshttps://doi.org/10.1007/s40415-026-01160-4openalex-snapshot
Microsatellite analysis sheds light on the conservation of Dyckia brevifolia Baker
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.104984openalex-snapshot
Responses to submergence and recovery in seedlings of the rheophyte Dyckia brevifolia (Bromeliaceae)
inferred← citeshttps://doi.org/10.1093/botlinnean/boaf038openalex-snapshot
Contrasting reproductive and ecological traits affect the genetic diversity and fine-scale genetic structure of two sympatric and epiphytic tropical bromeliads
inferred← citeshttps://doi.org/10.1093/botlinnean/boz099openalex-snapshot
Strong genetic structure in Dyckia excelsa (Bromeliaceae), an endangered species found on ironstone outcrops in Pantanal, Brazil
inferred← citeshttps://doi.org/10.1093/botlinnean/boz106openalex-snapshot
Population genetics shed light on species delimitation and life history of the Dyckia pernambucana complex (Bromeliaceae)
inferred← citeshttps://doi.org/10.1093/forsci/fxy026openalex-snapshot
Landscape Genetics and Genetic Conservation of Two Keystone Species from Ombrophilous Dense Forest: Euterpe edulis and Ocotea catharinensis
inferred← citeshttps://doi.org/10.1111/geb.70010openalex-snapshot
Global‐Scale Analysis Reveals Importance of Environment and Species Traits in Spatial Patterns of Riparian Plants' Genetic Diversity
inferred← citeshttps://doi.org/10.1111/plb.12847openalex-snapshot
Reproductive ecology ofOcotea catharinensis, an endangered tree species
inferred← citeshttps://doi.org/10.13057/biodiv/d210901openalex-snapshot
Inter-primer binding site (iPBS) markers reveal the population genetic diversity and structure of tropical climbing Cissampelopsis (Asteraceae) in Thailand
inferred← citeshttps://doi.org/10.15244/pjoes/91942openalex-snapshot
Pollination Biology of Hemiboea ovalifolia (Gesneriaceae), an Endangered Herb from Guangxi, China
inferred← citeshttps://doi.org/10.1590/1519-6984.278315openalex-snapshot
Demographic structure across all known populations of the rheophyte Dyckia brevifolia Baker (Bromeliaceae) in the Itajaí-Açu River, Southern Brazil
inferred← citeshttps://doi.org/10.1590/2175-7860202172116openalex-snapshot
Demographic structure of clonal, endemic, and endangered rheophyte bromeliad Dyckia ibiramensis: asexual vs sexual reproduction
inferred← citeshttps://doi.org/10.1590/2179-8087.080717openalex-snapshot
Genetic Diversity and Structure of Calophyllum brasiliense Along the Santa Catarina Coast
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2213650/v1openalex-snapshot
Demographic structure across all known populations of the rheophyte Dyckia brevifolia Baker (Bromeliaceae) in the Itajaí-Açú River, Southern Brazil
inferred← citeshttps://doi.org/10.3389/fpls.2021.626405openalex-snapshot
By Animal, Water, or Wind: Can Dispersal Mode Predict Genetic Connectivity in Riverine Plant Species?
inferred← citeshttps://doi.org/10.3390/f16050718openalex-snapshot
Reproductive Ecology of Lecythis Pisonis in Brazilian Agroforestry Systems: Implications for Conservation and Genetic Diversity
inferred← citeshttps://doi.org/10.3390/horticulturae8050390openalex-snapshot
In Vitro Germination and Propagation of Dyckia brevifolia, An Ornamental and Endangered Bromeliad
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